Read more about the article Isochromosome 17q10 associated with basophilia in primary myelofibrosis while with JAK2 inhibitor.
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Isochromosome 17q10 associated with basophilia in primary myelofibrosis while with JAK2 inhibitor.

Abstract

Continue ReadingIsochromosome 17q10 associated with basophilia in primary myelofibrosis while with JAK2 inhibitor.
Read more about the article Combinatorial Conflicting Homozygosity (CCH) analysis enables the rapid identification of shared genomic regions in the presence of multiple phenocopies.
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Combinatorial Conflicting Homozygosity (CCH) analysis enables the rapid identification of shared genomic regions in the presence of multiple phenocopies.

Abstract The ability to identify regions of the genome inherited with a dominant trait in one or more families has become increasingly valuable with the wide availability of high throughput…

Continue ReadingCombinatorial Conflicting Homozygosity (CCH) analysis enables the rapid identification of shared genomic regions in the presence of multiple phenocopies.
Read more about the article Effects of treatment with androgen receptor ligands on microRNA expression of prostate cancer cells.
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Effects of treatment with androgen receptor ligands on microRNA expression of prostate cancer cells.

Abstract Post-transcriptional regulation by microRNA (miRNA) is an important aspect of androgen receptor (AR) signalling in prostate cancer cells. However, the global profiling of miRNA expression in prostate cancer cells…

Continue ReadingEffects of treatment with androgen receptor ligands on microRNA expression of prostate cancer cells.
Read more about the article COL4A3/COL4A4 heterozygous mutations with TBMN presenting as focal segmental glomerulosclerosis.
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COL4A3/COL4A4 heterozygous mutations with TBMN presenting as focal segmental glomerulosclerosis.

Abstract

Continue ReadingCOL4A3/COL4A4 heterozygous mutations with TBMN presenting as focal segmental glomerulosclerosis.
Read more about the article Arrhythmic risk assessment in genotyped families with arrhythmogenic right ventricular cardiomyopathy.
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Arrhythmic risk assessment in genotyped families with arrhythmogenic right ventricular cardiomyopathy.

Abstract Arrhythmogenic right-ventricular cardiomyopathy (ARVC) is a genetically determined disorder, mostly caused by mutations in genes encoding desmosomal proteins. We evaluated phenotype/genotype characteristics to predict the risk for the first…

Continue ReadingArrhythmic risk assessment in genotyped families with arrhythmogenic right ventricular cardiomyopathy.
Read more about the article BRCA genetic screening in Middle Eastern and North African: mutational spectrum and founder BRCA1 mutation (c.798_799delTT) in North African.
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BRCA genetic screening in Middle Eastern and North African: mutational spectrum and founder BRCA1 mutation (c.798_799delTT) in North African.

Abstract The contribution of BRCA1 mutations to both hereditary and sporadic breast and ovarian cancer (HBOC) has not yet been thoroughly investigated in MENA. To establish the knowledge about BRCA1…

Continue ReadingBRCA genetic screening in Middle Eastern and North African: mutational spectrum and founder BRCA1 mutation (c.798_799delTT) in North African.
Read more about the article Phylogenetic relationships among four new complete mitogenome sequences of Pelophylax (Amphibia: Anura) from the Balkans and Cyprus.
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Phylogenetic relationships among four new complete mitogenome sequences of Pelophylax (Amphibia: Anura) from the Balkans and Cyprus.

Abstract We present the full-length mitogenome sequences of four European water frog species: Pelophylax cypriensis, P. epeiroticus, P. kurtmuelleri and P. shqipericus. The mtDNA size varied from 17,363 to 17,895 bp,…

Continue ReadingPhylogenetic relationships among four new complete mitogenome sequences of Pelophylax (Amphibia: Anura) from the Balkans and Cyprus.
Read more about the article Gene expression changes in HLA mismatched mixed lymphocyte cultures reveal genes associated with allorecognition.
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Gene expression changes in HLA mismatched mixed lymphocyte cultures reveal genes associated with allorecognition.

Abstract Human leucocyte antigen (HLA) compatibility is the main factor determining the occurrence of graft-vs-host disease (GVHD) in patients. It has also been shown that minor histocompatibility antigen differences as…

Continue ReadingGene expression changes in HLA mismatched mixed lymphocyte cultures reveal genes associated with allorecognition.
Read more about the article Molecular characterization and phylogeny of Kalotermes populations from the Levant, and description of Kalotermes phoeniciae sp. nov.
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Molecular characterization and phylogeny of Kalotermes populations from the Levant, and description of Kalotermes phoeniciae sp. nov.

Abstract The presence of the yellow-necked drywood termite, Kalotermes flavicollis Fabr., has been reported along most of the Mediterranean coasts of Europe, Africa and Asia. While morphological and genetic data…

Continue ReadingMolecular characterization and phylogeny of Kalotermes populations from the Levant, and description of Kalotermes phoeniciae sp. nov.
Read more about the article MicroRNA responses to environmental liver carcinogens: Biological and clinical significance.
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MicroRNA responses to environmental liver carcinogens: Biological and clinical significance.

Abstract A large number of biological, chemical, and dietary factors have been implicated in the development of liver cancer. These involve complex and protracted interactions between genetic, epigenetic, and environmental…

Continue ReadingMicroRNA responses to environmental liver carcinogens: Biological and clinical significance.